Spfkh1 encodes a transcription factor implicated in gut formation during sea urchin development

Development Growth and Differentiation

Volumn 39, Issue 3, 1997, Pages 285-294

  Luke, Natalie H ^a   Killian, Christopher E ^a,b   Livingston, Brian T ^a  

^a UNIVERSITY OF MISSOURI KANSAS CITY   (United States)

^b UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

Endoderm; Forkhead; Gene expression; Gut formation

Indexed keywords

DNA; MESSENGER RNA; TRANSCRIPTION FACTOR;

ADOLESCENT; ARTICLE; CELL MOTILITY; EMBRYO; EMBRYO DEVELOPMENT; ENDODERM; EXTRACELLULAR MATRIX; GENE EXPRESSION; INTESTINE; MALE; NONHUMAN; SEA URCHIN;

ECHINOIDEA;

EID: 0030951355     PISSN: 00121592     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1440-169X.1997.t01-2-00004.x     Document Type: Article

References (41)

1. Ang, S-L. & Rossant, J. 1994. HNF-3β is essential for node and notochord formation in mouse development. Cell 78, 561-574.
2. Ang, S.-L., Wierda, A., Wong, D. et al. 1993. The formation and maintenance of the definitive endoderm lineage in the mouse: Involvement of HNF3/forkhead proteins. Development 119, 1301-1315.
3. Azzaria, M., Goszczynski, B., Chung, M. A., Kalb, J. M. & McGhee, J. D. 1996. A forkhead/HNF-3 homologue expressed in the pharynx and intestine of the Caenorhabditis elegans embryo. Dev. Biol. 178, 289-303.
4. Benson, S., Rawson, R., Killian, C. & Wilt, F. 1991. Role of the extracellular matrix in tissue-specific gene expression in the sea urchin embryo. Mol. Reprod. Dev. 29, 220-226.
5. Benson, S. C., Sucov, H. M., Stephens, L., Davidson, E. H. & Wilt, F. 1987. A lineage-specific gene encoding a major matrix protein of the sea urchin embryo spicule. Dev. Biol. 120, 499-506.
6. Bolce, M. E., Hemmati-Brivanlou, A. & Harland, R. M. 1993. XFKH2, a Xenopus HNF-3α homologue, exhibits both activininducible and autonomous phases of expression in early embryos. Dev. Biol. 160, 413-423.
7. Cameron, R. A., Hough-Evans, B. R., Britten, R. J. & Davidson, E. H. 1987. Lineage and fate of each blastomere of the eight cell sea urchin embryo. Genes Dev. 1, 75-84.
8. Chen, S. W. & Wessel, G. M. 1996 Endoderm differentiation in vitro identifies a transitional period for endoderm ontogeny in the sea urchin embryo. Dev. Biol. 175, 57-65.
9. Childs, G., Maxson R. & Kedes, L. H. 1979. Histone gene expression during sea urchin embryogenesis: Isolation and characterization of early and late mRNA of S. purpuratus by gene specific hybridization and template activity. Dev. Biol. 73, 153-173.
10. Clark, K. L., Halay, E. D., Lai, E. & Burley, S. K. 1993. Co-crystal structure of the HNF-3/forkhead DMA-recognition motif resembles histone H5. Nature 364, 412-420.
11. Davidson, E. H. 1989. Lineage-specific gene expression and the regulative capacities of the sea urchin embryo: A proposed mechanism. Development 105, 421-445.
12. Davidson, E. H. 1991 Spatial mechanisms of gene regulation in metazoan embryos. Development 113, 1-26.
13. Ettensohn, C. A. & Ingersoll, E. P. 1992. Morphogenesis of the sea urchin embryo. In Morphogenesis: An Analysis of the Development of Biological Form (Eds E. F. Rossomando & S. Alexander) pp. 189-261. Marcel Dekker, New York.
14. Hall, H. G. 1978. Hardening of the sea urchin fertilization envelope by peroxide-catalyzed phenolic coupling of tyrosine. Cell 15, 342-355.
15. Hardin, J. 1989. Local shifts in position and polarized motility drive cell rearrangements during sea urchin gastrulation. Dev. Biol. 136, 430-445.
16. Harkey, M. A. & Whiteley, A. H. 1983. The program of protein synthesis during the development of the micromere-primary mesenchyme cell line in the sea urchin embryo. Dev. Biol. 100, 12-28.
17. Harkey, M. A., Whiteley, H. R. & Whiteley, A. H. 1992. Differential expression of the msp 130 gene among skeletal lineage cells in the sea urchin embryo: A three dimensional in situ hybridization analysis. Mech. Dev. 37, 173-184.
18. Hinegardner, R. 1967. Echinoderms. In Methods in Developmental Biology (Eds F. H. Wilt & N. K. Wessels), pp. 139-155. Crowell, New York.
19. Horstadius, S. 1973. Experimental Embryology of Echinoderms. Clarendon Press, Oxford.
20. Kaestner, K. H., Lee, K. H., Schlondorff, K-H., Heimisch. H., Monaghan, A. P. & Schutz, G. 1993. Six members of the mouse forkhead gene family are developmentally regulated. Proc. Natl Acad. Sci. USA 90, 7628-7631.
21. Lai, E., Prezioso, V. R., Tao, W., Chen, W. S. & Darnell, J. E. 1991. Hepatocyte nuclear factor 3a belongs to a gene family in mammals that is homologous to the Drosophila homeotic gene forkhead. Genes Dev. 5, 416-427
22. Lane, M. C., Koehl, M. A. R., Wilt, F. & Keller, R. 1993. A role for regulated secretion of apical extracellular matrix during invagination in the sea urchin. Development 117, 1049-1060.
23. Li, C. & Tucker, P. W. 1983. DNA-binding properties and secondary structural model of the hepatocyte nuclear factor 3/forkhead domain. Proc. Natl Acad. Sci. USA 90, 11583-11587.
24. Livingston, B. T. & Wilt, F. H. 1989. Lithium evokes expression of vegetal specific molecules in the animal blastomeres of sea urchin embryos. Proc. Natl Acad. Sci. USA 86, 3669-3673.
25. Livingston, B. T. & Wilt F. H. 1992. Phorbol esters alter cell fate during development of sea urchin embryos. J. Cell Biol. 119, 1641-1648.
26. Livingston, B. T. & Wilt, F. H 1995. Injection of myo-inositol reverses the effects of lithium on sea urchin blastomeres. Develop. Growth Differ. 37, 539-543.
27. Lutz, D. A. & Inoue, S. 1986. Techniques for observing living gametes and embryos Methods Cell Biol. 27, 90-109.
28. McClay, D. R. & Logan, C. Y. 1996). Regulative capacity of the archenteron during gastrulation in the sea urchin. Development 122, 607-616.
29. Melton, D. M., Kreig, P., Rebagliati, M., Maniatus, T, Zinn, K. & Green, M. 1984. Efficient in vitro synthesis of biologically active RNA and RNA hybridization probes from plasmids containing a bacteriophage SP6 promoter. Nucleic Acids Res. 12, 7035-7056.
30. Monaghan, A. P., Kaestner, K.,Grau, E. & Schutz, G. (1993). Postimplantation expression patterns indicate a role for the mouse forkhead/HNF-3α, β, and γ genes in determination of the definitive endoderm, chordamesoderm and neuroectoderm. Development 119, 567-578.
31. Nocente-McGrath, C., Mclsaac, R. & Ernst, S. G. 1991. Altered cell fate in LiCl-treated sea urchin embryos. Dev. Biol. 147, 445-450.
32. Pierrou, S., Hellqvist, M., Samuelsson, L., Enerback, S. & Carlsson, P. 1994. Cloning and characterization of seven human Forkhead Proteins: Binding site specificity and DNA bending. EMBO 13, 5002-5012.
33. Ransick, A. & Davidson, E. H. 1995. Micromeres are required for normal vegetal plate specification in sea urchin embryos. Development 121, 3215-3222.
34. Sasaki, H. & Hogan, B. L. M. 1993. Differential expression of multiple forkhead related genes during gastrulation and axial pattern formation in the mouse embryo. Development 118, 47-59.
35. Strahle. U., Blader, P., Henrique, D. & Ingham, P. W. 1993. Axial, a zebrafish gene expressed along the developing body axis, shows altered expression in Cyclops mutant embryos. Genes Dev. 7, 1436-1446.
36. Vlahou, A., Gonzalex-Rimbau, M. & Flytzanis, C. N. 1996. Maternal mRNA encoding the orphan steroid receptor SpCOUP-TF is localized in sea urchin eggs. Development 122, 521-526.
37. von Ubisch, L. 1929. Uber der determination der larvalen organe underder imaginalanlage beiseeigelen, Wilhelm Roux Arch. Entw. Mech. Org. 117, 81-122.
38. Weigel, D., Jurgens, G., Kuttner, F., Seifert, E. & Jackle, H. 1989. The homeotic gene forkhead encodes a nuclear protein and is expressed in the terminal regions of the Drosophila embryo. Cell 57, 645-658,
39. Weinstein, D. C., Altaba, A. R. I., Prezioso, W. S., Jessell, T. M. & Darnell, J. E. 1994. The winged-helix transcription factor HNF-3β is required for notochord development in the mouse embryo. Cell 78, 575-588.
40. Wessel, G. M., Goldberg, L., Lennarz, W. J. & Klein, W. H. 1989. Gastrulation in the sea urchin embryo is accompanied by the accumulation of an endoderm-specific mRNA. Dev. Biol. 136, 526-536.
41. Wessel, G. M. & McClay, D. R. 1987. Gastrulation in the sea urchin embryo requires the deposition of crosslinked collagen within the extracellular matrix. Dev. Biol. 121, 149-165.